US4826791A - Silicon carbide-alpha prime sialon beta prime sialon - Google Patents
Silicon carbide-alpha prime sialon beta prime sialon Download PDFInfo
- Publication number
- US4826791A US4826791A US07/056,096 US5609687A US4826791A US 4826791 A US4826791 A US 4826791A US 5609687 A US5609687 A US 5609687A US 4826791 A US4826791 A US 4826791A
- Authority
- US
- United States
- Prior art keywords
- sialon
- ceramic composite
- ceramic
- sic
- sic particles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 title 1
- 239000000919 ceramic Substances 0.000 claims abstract description 59
- 239000002131 composite material Substances 0.000 claims abstract description 46
- 239000002245 particle Substances 0.000 claims abstract description 42
- 239000011159 matrix material Substances 0.000 claims abstract description 29
- 238000005245 sintering Methods 0.000 claims description 20
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 description 22
- 239000000843 powder Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 6
- 238000001513 hot isostatic pressing Methods 0.000 description 6
- 238000000280 densification Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 3
- 238000007731 hot pressing Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 3
- 229910018404 Al2 O3 Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229910007277 Si3 N4 Inorganic materials 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052586 apatite Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000009694 cold isostatic pressing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910001719 melilite Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000001272 pressureless sintering Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/58—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
- C04B35/597—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon oxynitride, e.g. SIALONS
Definitions
- Prior art commercial SiC components such as seal rings, nozzles and bearings, while having high room temperature hardness, high abrasion resistance and high thermal conductivity, have poor fracture toughness, making them unsuitable for, or reducing their lifetime in, many applications where impact may occur.
- the range of useful applications of SiC components is further limited by the fabrication methods which are used to fabricate dense SiC articles. Fabrication of commercial SiC articles is performed by (1) hot pressing, which is a method that is usually only economical for relatively simple final component shapes; (2) sintering which, while allowing more complex shapes to be made, is also very costly due to the high temperatures (2000°-2300° C.) required to densify SiC; and (3) reaction bonding which, while capable of producing complex shapes, has inferior properties due to the presence of free silicon.
- Alpha prime-beta prime sialons are described in U.S. Pat. Nos. 4,563,433 and 4,547,470, and are exemplified by the commercial prior art composition, KYON 2000, which contains about 5 to 40 w/o (weight percent) alpha prime sialon, with the remainder being essentially beta prime sialon, except for minor phases which are mainly a result of sintering aid residues.
- KYON is a trademark of Kennametal Inc. for its ceramic compositions and articles.
- Beta prime sialon has the formula Si 6-z Al z O z N 8-z , where O ⁇ z ⁇ 5.
- Alpha prime sialon has the formula (Si,Al) 12 M x (O,N) 16 , where M is a sintering aid metal.
- a ceramic composite composition of very fine (1 micron or less average size) SiC particles in a beta prime sialon ceramic matrix is referred to in Richerson U.S. Pat. No. 3,890,250.
- SiC particles may be dispersed in an alpha prime/beta prime sialon matrix containing about 10 to about 67 w/o alpha prime sialon to provide improved hardness without having a significantly adverse affect on the fracture toughness of the material.
- the composite according to the present invention also has other properties, such as thermal conductivity, Young's modulus, abrasion resistance, thermal expansion coefficient which are increased compared with alpha prime-beta prime sialon.
- the present composite containing less than about 30 v/o SiC particles
- a ceramic composite containing 5 to 50 v/o SiC particles dispersed in a ceramic matrix.
- the SiC particles have a median size between about 1.5 to 15 microns, and preferably 2 to 9 microns.
- the ceramic matrix is essentially sialon.
- the sialon contains at least 10 w/o, and preferably, where high hardness and high toughness are desired, at least 50 w/o, alpha prime sialon, with the remainder being essentially beta prime sialon.
- the composite has a density of at least 3.1 g/cc, and preferably at least 3.15 g/cc.
- the alpha prime solution phase forms at least 60 w/o of the sialon in the ceramic matrix.
- alpha prime contents 10 to 50 w/o may be preferred.
- FIG. 1 is a photomicrograph (500 ⁇ ) of an as polished section through a ceramic composite in accordance with the present invention.
- FIG. 3 shows Rockwell A hardness of sintered and HIPped composites as a function of the ratio of alpha prime/beta prime sialon.
- FIG. 4 shows Rockwell A hardness as a function of the SiC content of the composite.
- FIG. 7 shows a longitudinal cross section through an annular seal ring in accordance with the present invention.
- SiC particles may be dispersed in a ceramic matrix containing alpha prime sialon to provide a ceramic composite that has high fracture toughness, high hardness and other enhanced properties.
- SiC particle size it has been found necessary to control the SiC particle size, the level of SiC in the ceramic composite, the amount of alpha prime sialon in the matrix, as well as the density of the final material.
- the level of SiC in the composite should be at least 5 v/o in order to obtain a minimal improvement in hardness.
- the hardness of the ceramic composite can be significantly improved (over that of commercial alpha prime-beta prime sialon-RA (Rockwell A) about 93.6) and may even approach that of commercial SiC (about 95 to 96 RA).
- SiC content should preferably not be increased beyond about 30 v/o. We believe that further increases in SiC content, while improving thermal and electrical conductivity, making it more readily electrodischarge machinable, will be accompanied by a reduction in sinterability (decreased densification) and toughness of the material.
- one or more minor phases are normally present in amounts of 0.1 to 10 w/o.
- These minor phases are typically intergranular and include a glassy or crystalline phase.
- yttria is used as the sintering aid, these minor phases may include YAG, N-YAM, Y-N-alpha-Wollastonite, B-phase, N-apatite and N-melilite.
- the ceramic composite is more difficult to densify during sintering, but we have also found that if too much minor phase is present, there will be a reduction in the useful properties of the ceramic composite. While not wishing to be bound by theory, we have theorized that the amount of minor phase present should be controlled within the foregoing range to form a very thin intergranular phase at least substantially encircling the SiC particles, and which we believe separates the SiC from the sialon. Therefore, for optimum results, we theorize that the amount of minor phase(s) desired is dependent upon the volume percent of SiC as well as the size of the SiC particles.
- the median size of the SiC particles it is, therefore, preferable to control the median size of the SiC particles to within the range of 1.5 to 15 microns.
- the average SiC particle size should be at least 1.5 microns.
- the upper limit of about 15 microns is believed to be necessary to assure an optimum hardening affect for a given volume of SiC particles. More preferably, the median size of the SiC particles should be between 2 and 9 microns.
- the level of alpha prime sialon in the sialon of the ceramic matrix is 10 to 67 w/o of the sialon present, with 33 to 90 w/o beta prime forming the remainder, of the sialon.
- the alpha prime content of the sialon should be at least 50 w/o, and more preferably, at least 60 w/o.
- Table I provides a listing of the compositions evaluated in Examples 1-5 which follow.
- the ceramic matrix powder mix utilized was: 83.8 w/o Si 3 N 4 -5.7 w/o AlN-3.9 w/o Al 2 O 3 -6.6 w/o Y 2 O 3 .
- the ceramic matrix powder mix utilized was: 85.5 w/o Si 3 N 4 -5.8 w/o AlN-4.0 w/o Al 2 O 3 -4.7 w/o Y 2 O 3 .
- the SiC starting powders were obtained from Lonza Ltd., Inorganic Chemical Division, CH-4002 Basel, Switzerland.
- the ceramic matrix powder mixture was premilled to obtain a median particle size of about 0.7 micron.
- the final powder blend for each mix (1 to 4) was then made by adding the necessary amount of SiC powder to the required weight of premilled ceramic matrix powder to produce 400 gm batches. These powders were then blended for 24 hours in a mill jar using 2 kilograms of sialon cycloids and 1 liter of isopropanol solvent. After blending, the powder was dried and then screened through a 40 mesh sieve. Green samples formed by cold isostatic pressing were subsequently sintered using conventional sialon sintering techniques at 1750° to 1850° C. for 1 hour under 1 atmosphere nitrogen.
- FIG. 1 A typical as polished microstructure of a composite made in accordance with the present invention is shown in FIG. 1.
- 25 v/o of substantially equiaxed SiC particles having a median size of 5.5 microns, are dispersed in a ceramic matrix (dark material) containing alpha prime sialon, beta prime sialon and minor phases due to sintering aid residues.
- Mixes 5-11 were processed in a manner similar to that detailed for Mixes 1-4, except that densification was achieved by hot pressing at a pressure of 5000 psi applied for about one-fourth hour at 1850° C.
- the material in accordance with the present invention may be utilized in those applications requiring both high wear resistance and high fracture resistance. It is specifically contemplated that the present invention can be utilized to make bearings and components for fluid handling systems such as nozzles and seal rings. Examples of conventional nozzle 60 and seal ring 70 geometries which may be made from the present composite are illustrated in FIGS. 6 and 7, respectively. In conjunction with the seal ring shown, it may be preferable to keep the alpha prime content within 10 to 50 w/o for optimum thermal conductivity.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Ceramic Products (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/056,096 US4826791A (en) | 1987-05-29 | 1987-05-29 | Silicon carbide-alpha prime sialon beta prime sialon |
| EP88904830A EP0346399B2 (fr) | 1987-05-29 | 1988-05-03 | Materiau ceramique composite et article ceramique produit |
| AU17966/88A AU1796688A (en) | 1987-05-29 | 1988-05-03 | Silicon carbide-alpha prime sialon |
| DE3877566T DE3877566T2 (de) | 1987-05-29 | 1988-05-03 | Keramisches verbundmaterial und daraus hergestellte gegenstaende. |
| PCT/US1988/001454 WO1988009313A1 (fr) | 1987-05-29 | 1988-05-03 | Carbure de silicium-sialon alpha prime |
| DE198888904830T DE346399T1 (de) | 1987-05-29 | 1988-05-03 | Werkstoff, bestehend aus alpha-tialon als grundstoff und aus siliciumkarbid. |
| CA000567533A CA1298321C (fr) | 1987-05-29 | 1988-05-24 | Carbure de silicium avec base d'alpha-sialon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/056,096 US4826791A (en) | 1987-05-29 | 1987-05-29 | Silicon carbide-alpha prime sialon beta prime sialon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4826791A true US4826791A (en) | 1989-05-02 |
Family
ID=22002121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/056,096 Expired - Lifetime US4826791A (en) | 1987-05-29 | 1987-05-29 | Silicon carbide-alpha prime sialon beta prime sialon |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4826791A (fr) |
| EP (1) | EP0346399B2 (fr) |
| AU (1) | AU1796688A (fr) |
| CA (1) | CA1298321C (fr) |
| DE (2) | DE346399T1 (fr) |
| WO (1) | WO1988009313A1 (fr) |
Cited By (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4987104A (en) * | 1986-03-14 | 1991-01-22 | Commonwealth Scientific & Industrial Research Organization | Method of forming a ceramic product |
| US5122485A (en) * | 1990-01-29 | 1992-06-16 | Nissan Motor Co., Ltd. | Sintered silicon carbide and silicon nitride base composite |
| US5196386A (en) * | 1989-09-18 | 1993-03-23 | The Tokyo Electric Power Company, Incorporated | Sintered ceramic composite body and method of manufacturing same |
| US5198165A (en) * | 1990-06-19 | 1993-03-30 | Nissan Motor Co., Ltd. | Sintered silicon carbide and sialon composite |
| US5217932A (en) * | 1989-09-18 | 1993-06-08 | The Tokyo Electric Power Co., Ltd. | Sintered ceramic composite body and method of manufacturing same |
| US5238885A (en) * | 1990-09-25 | 1993-08-24 | Kabushiki Kaisha Toshiba | Sialon type sintered bodies and method of producing the same |
| US5275986A (en) * | 1991-11-25 | 1994-01-04 | Sumitomo Electric Industries, Ltd. | Silicon nitride sintered body |
| US5298470A (en) * | 1989-09-22 | 1994-03-29 | The Carborundum Company | Silicon carbide bodies having high toughness and fracture resistance and method of making same |
| US5316856A (en) * | 1988-12-03 | 1994-05-31 | Ngk Spark Plug Co., Ltd. | Silicon nitride base sintered body |
| US5370716A (en) * | 1992-11-30 | 1994-12-06 | Kennamental Inc. | High Z sialon and cutting tools made therefrom and method of using |
| US5413972A (en) * | 1993-12-23 | 1995-05-09 | The Dow Chemical Company | SiAlON composites and method of preparing the same |
| US5459112A (en) * | 1994-09-14 | 1995-10-17 | The Carborundum Company | Reaction-bonded silicon carbide refractory product |
| US5521129A (en) * | 1994-09-14 | 1996-05-28 | The Carborundum Company | Sialon-bonded silicon carbide refractory |
| US5580510A (en) * | 1992-03-06 | 1996-12-03 | The Regents Of The University Of Michigan | Method for improving the toughness of silicon carbide-based ceramics |
| US5618768A (en) * | 1995-04-07 | 1997-04-08 | Honda Giken Kogyo Kabushiki Kaisha | Sintered body of silicon nitride and composite sintered body of silicon nitride and silicon carbide |
| WO1998023554A1 (fr) * | 1996-11-25 | 1998-06-04 | The Regents Of The University Of Michigan | CERAMIQUES A BASE DE SiAlON α RENFORCEES IN SITU |
| US5785922A (en) * | 1994-11-21 | 1998-07-28 | Honda Giken Kogyo Kabushiki Kaisha | Method for producing composite sintered body of silicon carbide and silicon nitride |
| US6124225A (en) * | 1998-07-29 | 2000-09-26 | The Regents Of The University Of Michigan | Cutting tools and wear resistant articles and material for same |
| WO2002044104A2 (fr) | 2000-11-28 | 2002-06-06 | Kennametal Inc. | Ytterbium contenant du sialon et procede de fabrication associe |
| US20020119017A1 (en) * | 2001-02-28 | 2002-08-29 | Gates Alfred S. | Oxidation-resistant cutting assembly |
| US20030134737A1 (en) * | 1997-10-20 | 2003-07-17 | Gerhard Wotting | Silicon nitride substances containing sintering additives and sio2, method for producing them and use of the same |
| US20040023035A1 (en) * | 2000-07-27 | 2004-02-05 | David Brandon | Wear and thermal resistant material produced from super hard particles bound in a matrix of glassceramic electrophoretic deposition |
| US20040033883A1 (en) * | 2000-11-28 | 2004-02-19 | Kennametal Inc. | SiA1ON containing ytterbium and method of making |
| WO2005016847A1 (fr) * | 2003-08-07 | 2005-02-24 | Ceramtec Ag Innovative Ceramic Engineering | Materiau a base de sialon |
| US20050189683A1 (en) * | 2000-11-28 | 2005-09-01 | Yeckley Russell L. | SiAION containing ytterbium and method of making |
| US20060178256A1 (en) * | 2005-02-09 | 2006-08-10 | Yeckley Russell L | SiAION ceramic and method of making the same |
| CN100448799C (zh) * | 2003-08-07 | 2009-01-07 | 创新陶瓷工程技术公司 | SiAlON基材料 |
| US7855159B1 (en) * | 2007-01-11 | 2010-12-21 | Kennametal Inc. | Alpha-beta SiAlON ballistic ceramic armor |
| EP2090557A3 (fr) * | 2008-02-13 | 2012-02-01 | NGK Insulators, Ltd. | Matériau d'oxyde d'yttrium, élément d'un dispositif pour la fabrication de semi-conducteurs, et procédé pour la préparation d'un matériau d'oxyde d'yttrium |
| US8367576B2 (en) | 2010-11-18 | 2013-02-05 | Kennametal Inc. | Charge-dispersing alpha prime-beta prime SiA1ON |
| US20150315088A1 (en) * | 2012-12-20 | 2015-11-05 | Xeracarb Limited | Sialon bonded silicon carbide material |
| EP2402098B2 (fr) † | 2004-12-22 | 2021-03-03 | Ngk Spark Plug Co., Ltd. | Insert en sialon et outil de découpe doté de celui-ci |
| US20230006373A1 (en) * | 2019-11-25 | 2023-01-05 | Continental Teves Ag & Co. Ohg | Electronics housing for automated assembly |
| US11906273B2 (en) | 2019-06-13 | 2024-02-20 | Kennametal Inc. | Armor plate, armor plate composite and armor |
| US12247811B2 (en) | 2022-01-12 | 2025-03-11 | Kennametal Inc. | Armor plate, armor plate composite and armor |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19730770C2 (de) * | 1996-08-06 | 2001-05-10 | Wacker Chemie Gmbh | Porenfreie Sinterkörper auf Basis von Siliciumcarbid, Verfahren zu ihrer Herstellung und ihre Verwendung als Substrate für Festplattenspeicher |
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| US3890250A (en) * | 1973-03-14 | 1975-06-17 | Norton Co | Hot pressed silicon nitride containing finely dispersed silicon carbide or silicon aluminum oxynitride |
| US3991166A (en) * | 1972-01-11 | 1976-11-09 | Joseph Lucas (Industries) Limited | Ceramic materials |
| US4127416A (en) * | 1976-07-24 | 1978-11-28 | Lucas Industries Limited | Method of producing a ceramic product |
| US4184882A (en) * | 1976-03-25 | 1980-01-22 | Westinghouse Electric Corp. | Silicon nitride-silicon carbide composite material |
| US4547470A (en) * | 1983-04-25 | 1985-10-15 | Mitsubishi Kinzoku Kabushiki Kaisha | Sialon-base ceramic materials excellent in wear resistance |
| GB2157282A (en) * | 1984-04-06 | 1985-10-23 | Santrade Ltd | Nitride-based ceramic material |
| JPS60246268A (ja) * | 1984-05-23 | 1985-12-05 | 三菱マテリアル株式会社 | サイアロン基セラミツクス |
| JPS60260471A (ja) * | 1984-06-04 | 1985-12-23 | 新技術事業団 | β―サイアロンを含まないα―サイアロン質焼結体 |
| US4563433A (en) * | 1982-02-22 | 1986-01-07 | Kennametal Inc. | Ceramic material and method of manufacture |
| US4594106A (en) * | 1983-02-22 | 1986-06-10 | Tateho Kagaku Kogyo Kabushiki Kaisha | Spraying materials containing ceramic needle fiber and composite materials spray-coated with such spraying materials |
| JPS61291463A (ja) * | 1985-06-17 | 1986-12-22 | 日本特殊陶業株式会社 | 高靭性セラミツク工具用材料 |
-
1987
- 1987-05-29 US US07/056,096 patent/US4826791A/en not_active Expired - Lifetime
-
1988
- 1988-05-03 DE DE198888904830T patent/DE346399T1/de active Pending
- 1988-05-03 DE DE3877566T patent/DE3877566T2/de not_active Expired - Lifetime
- 1988-05-03 AU AU17966/88A patent/AU1796688A/en not_active Abandoned
- 1988-05-03 EP EP88904830A patent/EP0346399B2/fr not_active Expired - Lifetime
- 1988-05-03 WO PCT/US1988/001454 patent/WO1988009313A1/fr not_active Ceased
- 1988-05-24 CA CA000567533A patent/CA1298321C/fr not_active Expired - Fee Related
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US3991166A (en) * | 1972-01-11 | 1976-11-09 | Joseph Lucas (Industries) Limited | Ceramic materials |
| US3890250A (en) * | 1973-03-14 | 1975-06-17 | Norton Co | Hot pressed silicon nitride containing finely dispersed silicon carbide or silicon aluminum oxynitride |
| US4184882A (en) * | 1976-03-25 | 1980-01-22 | Westinghouse Electric Corp. | Silicon nitride-silicon carbide composite material |
| US4127416A (en) * | 1976-07-24 | 1978-11-28 | Lucas Industries Limited | Method of producing a ceramic product |
| US4127416B1 (fr) * | 1976-07-24 | 1984-10-30 | ||
| US4563433A (en) * | 1982-02-22 | 1986-01-07 | Kennametal Inc. | Ceramic material and method of manufacture |
| US4594106A (en) * | 1983-02-22 | 1986-06-10 | Tateho Kagaku Kogyo Kabushiki Kaisha | Spraying materials containing ceramic needle fiber and composite materials spray-coated with such spraying materials |
| US4547470A (en) * | 1983-04-25 | 1985-10-15 | Mitsubishi Kinzoku Kabushiki Kaisha | Sialon-base ceramic materials excellent in wear resistance |
| GB2157282A (en) * | 1984-04-06 | 1985-10-23 | Santrade Ltd | Nitride-based ceramic material |
| JPS60246268A (ja) * | 1984-05-23 | 1985-12-05 | 三菱マテリアル株式会社 | サイアロン基セラミツクス |
| JPS60260471A (ja) * | 1984-06-04 | 1985-12-23 | 新技術事業団 | β―サイアロンを含まないα―サイアロン質焼結体 |
| JPS61291463A (ja) * | 1985-06-17 | 1986-12-22 | 日本特殊陶業株式会社 | 高靭性セラミツク工具用材料 |
Cited By (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4987104A (en) * | 1986-03-14 | 1991-01-22 | Commonwealth Scientific & Industrial Research Organization | Method of forming a ceramic product |
| US5316856A (en) * | 1988-12-03 | 1994-05-31 | Ngk Spark Plug Co., Ltd. | Silicon nitride base sintered body |
| US5196386A (en) * | 1989-09-18 | 1993-03-23 | The Tokyo Electric Power Company, Incorporated | Sintered ceramic composite body and method of manufacturing same |
| US5217932A (en) * | 1989-09-18 | 1993-06-08 | The Tokyo Electric Power Co., Ltd. | Sintered ceramic composite body and method of manufacturing same |
| US5298470A (en) * | 1989-09-22 | 1994-03-29 | The Carborundum Company | Silicon carbide bodies having high toughness and fracture resistance and method of making same |
| US5122485A (en) * | 1990-01-29 | 1992-06-16 | Nissan Motor Co., Ltd. | Sintered silicon carbide and silicon nitride base composite |
| US5198165A (en) * | 1990-06-19 | 1993-03-30 | Nissan Motor Co., Ltd. | Sintered silicon carbide and sialon composite |
| US5238885A (en) * | 1990-09-25 | 1993-08-24 | Kabushiki Kaisha Toshiba | Sialon type sintered bodies and method of producing the same |
| US5275986A (en) * | 1991-11-25 | 1994-01-04 | Sumitomo Electric Industries, Ltd. | Silicon nitride sintered body |
| US5580510A (en) * | 1992-03-06 | 1996-12-03 | The Regents Of The University Of Michigan | Method for improving the toughness of silicon carbide-based ceramics |
| US5370716A (en) * | 1992-11-30 | 1994-12-06 | Kennamental Inc. | High Z sialon and cutting tools made therefrom and method of using |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO1988009313A1 (fr) | 1988-12-01 |
| DE3877566T2 (de) | 1996-04-11 |
| DE3877566D1 (de) | 1993-02-25 |
| EP0346399B1 (fr) | 1993-01-13 |
| EP0346399A1 (fr) | 1989-12-20 |
| EP0346399B2 (fr) | 1995-08-30 |
| DE346399T1 (de) | 1990-05-23 |
| EP0346399A4 (en) | 1990-09-05 |
| CA1298321C (fr) | 1992-03-31 |
| AU1796688A (en) | 1988-12-21 |
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